Nur, Hadi and Wei, Lim Kheng and Endud, Salasiah (2009) Hydrolyzed octadecyltrichlorosilane functionalized with amino acids as heterogeneous enantioselective catalysts. Reaction Kinetics and Catalysis Letters, 98 (1). pp. 157-164. ISSN 0133-1736
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Official URL: http://dx.doi.org/10.1007/s11144-009-0056-7
Abstract
Heterogeneous asymmetric catalysts using amino acids as chiral promoter were synthesized by attachment of amino acids such as l-glutamic acid and l-phenylalanine onto the hydrophilic part of hydrolyzed octadecyltrichlorosilane (OTS). The catalysts exhibited 12-18% enantiomeric excess (ee) for the asymmetric hydration of epoxycyclohexene to yield (1R,2R)-trans-1,2- cyclohexanediol and (1S,2S)-trans-1,2-cyclohexanediol.
Item Type: | Article |
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Uncontrolled Keywords: | amino acid as chiral promoter, asymmetric hydration of epoxycyclohexene, heterogeneous asymmetric catalysts |
Subjects: | Q Science > QD Chemistry |
Divisions: | Science |
ID Code: | 14913 |
Deposited By: | Zalinda Shuratman |
Deposited On: | 30 Sep 2011 15:12 |
Last Modified: | 07 May 2017 06:17 |
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